CN108128765B - Method for preparing nitrogen-doped porous carbon material and application - Google Patents
Method for preparing nitrogen-doped porous carbon material and application Download PDFInfo
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- CN108128765B CN108128765B CN201711435506.5A CN201711435506A CN108128765B CN 108128765 B CN108128765 B CN 108128765B CN 201711435506 A CN201711435506 A CN 201711435506A CN 108128765 B CN108128765 B CN 108128765B
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- 238000000034 method Methods 0.000 title claims abstract description 30
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- 239000002608 ionic liquid Substances 0.000 claims abstract description 68
- 239000002243 precursor Substances 0.000 claims abstract description 62
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- 239000000783 alginic acid Substances 0.000 claims abstract description 31
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 18
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- 239000000463 material Substances 0.000 claims description 27
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- 229940072056 alginate Drugs 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 72
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N N,N-Diethylethanamine Substances CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
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- 238000004566 IR spectroscopy Methods 0.000 description 1
- -1 KOH activated nitrogen Chemical class 0.000 description 1
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- 238000001069 Raman spectroscopy Methods 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
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- DLGYNVMUCSTYDQ-UHFFFAOYSA-N azane;pyridine Chemical compound N.C1=CC=NC=C1 DLGYNVMUCSTYDQ-UHFFFAOYSA-N 0.000 description 1
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- DOTMOQHOJINYBL-UHFFFAOYSA-N molecular nitrogen;molecular oxygen Chemical compound N#N.O=O DOTMOQHOJINYBL-UHFFFAOYSA-N 0.000 description 1
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- 229910052698 phosphorus Inorganic materials 0.000 description 1
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- 229920000642 polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
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- 238000012360 testing method Methods 0.000 description 1
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- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/26—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
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- H—ELECTRICITY
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- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/84—Processes for the manufacture of hybrid or EDL capacitors, or components thereof
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- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
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Abstract
The invention discloses a method for preparing a nitrogen-doped porous carbon material and application thereof. The invention is based on the existence of carboxyl in alginic acid molecular structure, utilizes the reaction of carboxyl and organic alkali with different structures to prepare a series of alginic acid proton type ionic liquid, has mild reaction, can adjust the structure of the alginic acid proton type ionic liquid through the structure regulation and control of the organic alkali very simply and conveniently, achieves the purpose of regulating and controlling the nitrogen content and the nitrogen species in the nitrogen-doped porous carbon material and the precursor thereof, carries out in-situ nitrogen doping on alginic acid from the molecular level, solves the key problem that a carbon source and a nitrogen source are uncontrollable, further realizes high-value utilization of the prepared nitrogen-containing carbon material, successfully takes the alginic acid base nitrogen-containing carbon material as an electrode material alone, and is successfully applied to the field of energy storage.
Description
Technical Field
The invention relates to the technical field of material science, in particular to a method for preparing a nitrogen-doped porous carbon material and application thereof.
Background
The development of human society and the rapid consumption of traditional energy have led people to pay attention to clean energy, and supercapacitors are widely applied to numerous fields such as intelligent wearing and new energy automobiles due to the advantages of rapid charging and discharging, high power density, long cycle life and the like. The carbon material has the characteristics of high specific area, excellent conductivity, controllable aperture, low price and the like, and becomes a main material of capacitor electrodes (a), LIU, A.Y. and M.L. COHEN, Science,1989.245(4920): p.841-842; b) xia, Y.and R.Mokaya, Advanced Materials,2004.16(17): p.1553-1558.). The synthesis of carbon materials with high energy density and cycle life to meet practical applications has become a hotspot of research today. A large number of researches show that the doping of the heteroatom (such as phosphorus, nitrogen, sulfur, greenhouse and the like) can not only improve the wettability of the carbon material and the electrolyte, but also effectively improve the specific capacity and the conductivity of the carbon material. Nitrogen atoms are close to carbon atoms in atomic radius and therefore do not contribute substantially to the material structure (a) Goettmann, f., et al., angelwald Chemie International Edition,2006.45(27): p.4467-4471); b) zheng, y., et al, Energy & Environmental Science,2012.5(5): p.6717-6731). The traditional nitrogen doping method is generally characterized in that a carbon source and a nitrogen source are mixed to obtain a nitrogen-containing carbon material, and the precursor synthesis process is complex and poor in plasticity. The search for an environment-friendly, efficient and simple precursor synthesis method to prepare nitrogen-containing carbon materials is an urgent requirement for the development of electrode materials.
The amount of seaweed in marine life is very large and the number and variety of seaweeds is large. Alginic acid (
O.and g.trends in Biotechnology,1990.8, 71-78.) is a natural polysaccharide high molecular polymer extracted from brown algae, alginic acid exists mainly in the form of calcium salt and sodium salt in plant cells of brown algae, plays a role in strengthening cell walls in the cells, and the content of sodium alginate in dried brown algae is generally about 20%, so we also refer to alginic acid as alginic acid (Haug, a., b.larsen, and O) many times.
Carbohydrate Research,1974.32(2): p.217-225.). Because of its low price, it is widely used as carbon source to prepare carbon material, and the synthesized carbon material has high conductivity and specific capacity. However, the problems of the traditional method for preparing the carbon material by utilizing alginic acid are as follows:
(1) the specific surface area is low, and the performance of the prepared carbon material is relatively low (Tian, Z.W., et al, Materials Letters,2016.180: p.162-165.).
(2) Alginic acid produces carbon Materials only as supports for metal Materials (a) Papageorgiou, S.K., et al, Journal of Hazardous Materials,2011.189(1): p.384-390; b) wang, N., et al, Acs Applied Materials & Interfaces,2016.8(25): p.16035-16044.).
(3) Alginic acid is used as a Carbon source to be mixed with nitrogen sources such as urea and the like to prepare nitrogen-containing Carbon materials, and the nitrogen doping amount and the precursor can not be controllably prepared (a) Sa, V.and K.G.Kornev, Carbon,2011.49(6): p.1859-1868.; b) xuan, C, et al, Chemcathem, 2017.9(5): p.809-815.), 2017.10.10, the Chinese patent office protected a nitrogen-oxygen co-doped hierarchical porous carbon derived from polyaniline-sodium alginate hydrogel with patent number CN 105480963B and a preparation method thereof.
The ionic liquid is a liquid substance completely composed of anions and cations at room temperature or near room temperature, and is widely applied to the preparation of nitrogenous carbon Materials (a) Paraknowtsch, J.P., et al, Advanced Materials,2010.22(1): p.87- +, due to the characteristics of low vapor pressure, good thermal stability, wide liquid range, various types and the like; b) zhang, S.G., et al, Journal of the American Chemical Society,2014.136(5): p.1690-1693.). The traditional ionic liquid has high price and complex synthesis process, and the like, so that the preparation of the industrial carbon material is limited.
Disclosure of Invention
Aiming at the defects of the prior art, the invention provides a method for preparing a nitrogen-doped porous carbon material and application thereof, and the method has the advantages of efficient preparation efficiency and simple and convenient production mode, so as to overcome the defects of the prior art.
In order to achieve the purpose, the invention is realized by the following technical scheme: the method for preparing the nitrogen-doped porous carbon material by using the alginic acid proton type ionic liquid as the precursor comprises the following steps:
1) mixing alginic acid, organic alkali and water, and reacting at 20-100 deg.C for 0.1-48 hr to synthesize alginic acid proton type ionic liquid solution;
2) drying the alginic acid proton type ionic liquid solution to obtain alginic acid proton type ionic liquid;
3) activating by using alginic acid proton type ionic liquid as a precursor through a direct carbonization method or a two-step carbonization method to obtain a nitrogen-doped carbon material product;
4) and (3) continuously washing the nitrogen-doped carbon material product by hydrochloric acid and pure water, and drying at 50-150 ℃ under reduced pressure to obtain the nitrogen-doped porous carbon material.
The specific chemical structure of the alginic acid is as follows:
where 50< n < 1000.
The organic base has the following structural formula:
the molar ratio of the organic alkali to the alginic acid is 0.5-2: 1; the mass concentration of the formed alginic acid proton type ionic liquid in the solution is 20-80%, and the specific reaction is as follows:
the drying in step 2) is at-20-Drying at 50 deg.C for 1-48 hr; the dried alginic acid proton type ionic liquid comprises anions and cations; the anion has the structural formula:
wherein 50< n < 1000;
the cation has the structural formula:
the direct carbonization method in the step 3) is specifically that the alginic acid proton type ionic liquid is transferred into a tubular furnace for heat treatment, the heating rate is 5-10 ℃/min, the inert gas is argon, the argon flow is 300mL/min, the carbonization temperature is 700-1000 ℃, and the heat preservation time is 0.5-5 h.
The two-step carbonization method in the step 3) comprises the following steps:
a) transferring the alginic acid proton type ionic liquid powder into a tubular furnace for primary sintering, wherein the heating rate is 5-10 ℃/min, the inert gas is argon, the argon flow is 300mL/min, the carbonization temperature is 400-500 ℃, and the heat preservation time is 0.5-2 h; obtaining a preliminary sintered carbon material;
b) mixing the primary sintered carbon material obtained in the step a) with a pore-forming agent, and carrying out pore-forming while carbonizing, wherein the pore-forming agent is potassium hydroxide, and the mass ratio of the carbon material to the potassium hydroxide is 1: 1-1: 5, the heating rate is 5-10 ℃/min, the inert gas is argon, the argon flow is 300ml/min, the carbonization temperature is 700-900 ℃, and the heat preservation time is 1-5 h.
In the step 4), the activated carbon material cleaning solution is 2M hydrochloric acid solution, and the amount of the hydrochloric acid solution is 5-10 times of the mass of the carbon material; the cleaning time is 1-10h, then cleaning for 2-5 times with pure water of 10-50 times of the mass, the reduced pressure drying temperature is 50-150 ℃, and the drying time is 1-5 h.
The nitrogen-doped porous carbon material is applied as an electrode.
In order to verify the technical effect of the present invention, the applicant conducted the following experiments:
preparation of nitrogen-doped porous carbon material
1. The preparation method is the same as above.
The inventors confirmed by infrared as shown in fig. 2.
2. Preparation of nitrogen-doped porous carbon material
Under the protection of argon, placing alginic acid proton type ionic liquid powder in a tube furnace, heating to 700-1000 ℃ (the heating rate is 5-10 ℃/min), carbonizing for 1-3 h, the argon flow is 100-.
3. Preparation of KOH activated nitrogen doped porous carbon material
Putting alginic acid proton type ionic liquid powder into a tube furnace under the protection of argon, heating to 500 ℃ (the heating rate is 5-10 ℃/min), presintering for 1h, naturally cooling to room temperature, taking out a sample, grinding into powder, and mixing with the following components in percentage by weight of 4: 1, mixing and grinding with KOH. And under the protection of argon, putting the mixture into a tube furnace, heating to 700-900 ℃ (the heating rate is 5-10 ℃/min), carbonizing for 2h, cooling to room temperature, taking out the sample, cleaning with 2M hydrochloric acid, cleaning with pure water for 3 times, and vacuum drying at 110 ℃ for 6h to obtain the KOH-activated nitrogen-containing carbon material, wherein the label is A-X-NDPs-Y-4, X is a carbonization precursor, and Y is the carbonization temperature.
Characterization of nitrogen-doped porous carbon structure
1. Infrared Spectroscopy (FT-IR)
In FIG. 2, a represents alginic acid (A), b represents a proton type ionic liquid spectrum of alginic acid-tetramethylguanidine (A-TMG), c represents an infrared spectrum of alginic acid-1, 8-diazabicycloundecen-7-ene (A-DBU) proton type ionic liquid, d represents an infrared spectrum of alginic acid-triethylamine (A-TEA) proton type ionic liquid, and e represents an infrared spectrum of alginic acid-1-methylimidazole (A-1-Mi) proton type ionic liquid. As can be seen from FIG. 2, at 1739cm-1The absorption band at (A) is generated by stretching vibration of C ═ O in COOH on alginic acid, 1608cm-1 in b, C, d and e is generated by vibration of C ═ O in C00-, and the absorption peak at 1739 disappears, which shows that carboxyl groups in alginic acid are largely deprotonated to generate COO-, thereby generating ionic bonds with cations in organic base to generate corresponding alginic acid proton type ionic liquid.
2. Analysis of Raman spectra
In FIG. 3, a represents the ratio of A-TEA proton type ionic liquid precursor to KOH at 1: 4 at 900 deg.c, b represents a pre-sintered 1h of a-TMG proton type ionic liquid precursor at 500 deg.c, with KOH at a ratio of 1: 4 at 900 ℃, c represents that after presintering the A-1-Mi proton type ionic liquid precursor for 1h at 500 ℃, the precursor is mixed with KOH in a proportion of 1: 4 at 900 ℃, d represents that after the A-DBU proton type ionic liquid precursor is presintered for 1h at 500 ℃, the precursor is mixed with KOH in a proportion of 1: 4 is activated at 900 ℃ to prepare (A-DBU-NDPs-900-4), and both the D-peak and the G-peak are Raman characteristic peaks of a C atom crystal, and are respectively in the vicinity of 1300cm < -1 > and 1580cm < -1 >. The D-peak represents a defect of a lattice of C atoms, and the G-peak represents an in-plane stretching vibration of a hybridization of a C atom sp 2. This peak is the fundamental vibration mode of graphite crystals, whose intensity is related to the size of the crystals, from fig. 3 it can be seen that we prepared graphitizing different nitrogen-containing carbon materials from different precursors.
In FIG. 4, a represents the ratio of A-TMG proton type ionic liquid precursor to KOH at 1: the mass ratio of 4 is activated at 900 ℃ to prepare (A-TMG-NDPs-900-4), b represents that the A-TMG proton type ionic liquid precursor is directly carbonized at 900 ℃ to prepare (A-TMG-NDPs-900), and the carbon material after distributed activation has a better graphitized structure.
3. Energy spectrum analysis and element analysis
FIG. 5 is a general spectrum of carbon materials of A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4, in FIG. 6, a is an enlarged view of the nitrogen spectrum of A-TEA-NDPs-900-4, b is an enlarged view of the nitrogen spectrum of A-TMG-NDPs-900-4, c is an enlarged view of the nitrogen spectrum of A-1-Mi-NDPs-900-4, and d is an enlarged view of the nitrogen spectrum of A-DBU-NDPs-900-4. As can be seen from the figure, the nitrogen-containing carbon materials prepared from different precursors not only have different nitrogen contents, but also have different nitrogen existing forms such as graphite nitrogen, pyridine nitrogen and the like. From elemental analysis, the unactivated carbon material has a high nitrogen content of 7.25% and a high nitrogen content of 1.14% after activation, and more importantly, carbon materials prepared from different precursors have different nitrogen and other element contents.
Third, characterization of electrochemical properties of doped porous carbon
The electrochemical performance of the prepared material is tested by adopting Cyclic Voltammetry (CV), constant current charging and discharging (GCD), alternating current impedance spectroscopy (EIS) and cyclic life.
FIG. 7 shows the sample concentration at 1mol/L Et4NBF4Cyclic voltammetry tests of different carbon materials in AN organic symmetric supercapacitor. As can be seen from the graph, the CV curve of the carbon material produced was substantially rectangular, and neither oxidation nor reduction was observedThe original peak shows that the material not only has a good electrochemical stability window but also has good reversibility under the high voltage of 0-2.7V.
FIG. 8 shows carbon materials prepared from different precursors at 1mol/L Et in the present invention4NBF4In the/AN organic symmetrical super capacitor, a 4A/g large current constant current charging and discharging (GCD) curve is adopted. FIG. 8 shows that all carbon materials are almost symmetrical isosceles triangles in the voltage range of 0-2.7V, which indicates that the prepared material has good reversibility and high coulombic efficiency, has high specific capacity under high-current charge and discharge, and is up to 125F/g, which is greatly improved compared with the previously reported carbon materials.
FIG. 9 is an AC impedance spectrum of the electrode material of the present invention. The spectrogram consists of two parts, namely a curve of a high-frequency region and a straight line of a low-frequency region, and the material under the high-frequency region has smaller resistance and minimum 0.3 omega, which indicates that the material has good conductivity and electron transmission speed.
FIG. 10 is a graph showing the cycle life of the material of the present invention in a 1mol/L Et4NBF4/AN organic symmetric supercapacitor, and it can be seen from FIG. 10 that the capacity fading is less after 5000 times of constant current charging and discharging cycles at a high current of 4A/g, and the A-TEA-NDPs-900-4 has only 3% capacity fading, which indicates that the material stability is excellent. While A-DBU-NDPs-900-4 may have a large capacity fade due to collapse of the pore size during cycling.
In summary, the invention uses alginic acid proton type ionic liquid as a nitrogen-containing precursor, and solves the problem that the nitrogen content and the existence form in the preparation of the nitrogen-containing carbon material from a carbon source and a carbon source are uncontrollable through the processes of pre-sintering and carbonization activation, so that the nitrogen-containing carbon material with high electrochemical performance is prepared, and the prepared material has different graphitization, nitrogen content and nitrogen existence form, thereby successfully realizing the regulation and control of the precursor material on the structure of the carbon-containing material. Therefore, the invention provides a new method for preparing the nitrogenous carbon material by efficiently utilizing alginic acid at the molecular level.
Advantageous effects
Compared with the prior art, the method is based on the existence of carboxyl in the molecular structure of alginic acid, utilizes the reaction of the carboxyl and organic alkali with different structures to prepare a series of alginic acid proton type ionic liquid, has mild reaction, can adjust the structure of the alginic acid proton type ionic liquid through the structural regulation and control of the organic alkali very simply and conveniently, achieves the purpose of regulating and controlling the nitrogen content and the nitrogen species in the nitrogen-doped porous carbon material and the precursor thereof, carries out in-situ nitrogen doping on alginic acid from the molecular level, solves the key problem of uncontrollable carbon source and nitrogen source, further realizes high-value utilization of the prepared nitrogen-containing carbon material, successfully takes the alginic acid base nitrogen-containing carbon material as an electrode material independently, and is successfully applied to the field of energy storage.
Drawings
FIG. 1 shows the synthesis method of alginic acid proton type ionic liquid precursor and the available organic base;
FIG. 2 is an infrared spectrum of the precursors A, A-TMG, A-DBU, A-TEA and A-1-Mi;
FIG. 3 is a Raman spectrum of A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4 synthesized by activation of different precursors;
FIG. 4 is a Raman spectrum of A-DBU-NDPs-900 before activation and A-DBU-NDPs-900-4 after activation with KOH;
FIG. 5 is a general diagram of the spectra of A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4 synthesized by different precursor activation;
FIG. 6 is an enlarged view of the spectrum of N1s in A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4 synthesized by different precursor activation;
FIG. 7 is a Cyclic Voltammogram (CV) at a sweep rate of 20mv/s for A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4, and A-1-Mi-NDPs-900-4 synthesized by different precursor activation;
FIG. 8 is a constant current charge/discharge curve (GCD) at 4A/g current density for A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4 synthesized by different precursor activation;
FIG. 9 is a diagram showing conventional impedance spectra of A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4 synthesized by different precursor activation;
FIG. 10 shows the cycle life of A-TMG-NDPs-900-4, A-DBU-NDPs-900-4, A-TEA-NDPs-900-4 and A-1-Mi-NDPs-900-4 synthesized by different precursor activation, which cycles 5000 times under 4A/g constant current charging and discharging.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1 of the invention: preparation of alginic acid-1, 8-diazabicycloundecen-7-ene proton type ionic liquid precursor (A-DBU): 34.576g of DBU were weighed into a 250ml flask, 100ml of pure water were added, and 40g of alginic acid were added after complete mixing. Reacting at 25 ℃ for 12h, and drying the solution by a freeze dryer for 48 h. And crushing the mixture into powder by using a crusher to prepare the A-DBU alginic acid proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-1, 8-diazabicycloundecen-7-ene proton type ionic liquid precursor is directly put into a tube furnace, and the precursor is directly heated to 900 ℃ under the Ar condition for carbonization, wherein the heating rate is 5 ℃/min, the carbonization time is 2h, and the argon flow is 200 ml/min. And (3) taking out a sample after the temperature is reduced to normal temperature to obtain a target product-A-DBU-NDPs-900, wherein the yield is 16.7%, the nitrogen content of the obtained material is high with the nitrogen content of 7.25%, and the specific capacity of the obtained material is 44F/g when the graphitization degree is ID/IG (identity/oxygen) is 1.07.
Example 2 of the invention: preparation of alginic acid-1, 8-diazabicycloundecen-7-ene proton type ionic liquid precursor (A-DBU): 34.576g of DBU were weighed into a 250ml flask, 100ml of pure water were added, and 40g of alginic acid were added after complete mixing. Reacting for 8h at 40 ℃, and drying the solution for 48h by using a freeze dryer. And crushing the mixture into powder by using a crusher to prepare the A-DBU alginic acid proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-1, 8-diazabicycloundecen-7-ene proton type ionic liquid precursor is put into a tube furnace to be carbonized for 1h at 500 ℃ under the Ar condition, the heating rate is 5 ℃/min, the argon flow is 200ml/min, after the temperature is reduced to the room temperature, 1.75g of a sample is weighed, 1.5g of the sample is weighed and mixed with 6g of KOH for grinding, and the proportion of KOH/sample is 4: 1, activating the carbon material at 900 ℃ for 2 h. The temperature rise rate was 5 ℃/min and the argon flow rate was 200 ml/min. After a sample is taken out, residual KOH is washed away by using 2M HCl, the sample is washed for 3 times by using pure water, and the sample is dried for 6 hours in vacuum at 110 ℃ to obtain a target product-A-DBU-NDPs-900-4, wherein the yield is 8.74%, the nitrogen content of the obtained material is high and 1.19%, the graphitization degree is that ID/IG is 0.99, and the specific capacity is 125F/g under the current density of 4A/g.
Example 3 of the invention: preparation of alginic acid-1, 8-diazabicycloundecen-7-ene alginic acid proton type ionic liquid precursor (A-DBU): 34.576g of DBU were weighed into a 250ml flask, 100ml of pure water were added, and 40g of alginic acid were added after complete mixing. Reacting at 100 ℃ for 12h, and drying the solution by a freeze dryer for 48 h. And crushing the mixture into powder by using a crusher to prepare the A-DBU alginic acid proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-1, 8-diazabicycloundecan-7-ene alginic acid proton type ionic liquid precursor is put into a tube furnace to be carbonized for 1h at 500 ℃ under the Ar condition, the heating rate is 5 ℃/min, the argon flow is 200ml/min, after the temperature is reduced to the room temperature, 1.75g of a sample is weighed, 1.5g of the sample is weighed and mixed with 6g of KOH for grinding, and the proportion is that KOH/sample is 4: 1, activating the carbon material at 800 ℃ for 2 h. The temperature rise rate was 5 ℃/min and the argon flow rate was 200 ml/min. After a sample is taken out, residual KOH is washed away by using 2M HCl, the sample is washed for 3 times by using pure water, and the sample is dried for 6 hours in vacuum at 110 ℃ to obtain a target product-A-DBU-NDPs-900-4, wherein the yield is 11.96%, the nitrogen content of the obtained material is high and 1.46%, the graphitization degree is that ID/IG is 1.00, and the specific capacity is 102F/g under the current density of 4A/g.
Example 4 of the invention:
preparation of alginic acid-1, 8-diazabicycloundecen-7-ene alginic acid proton type ionic liquid precursor (A-DBU): weighing 69.0g of DBU, putting the DBU into a 250ml flask, adding 100ml of pure water, and adding 40g of alginic acid after completely mixing; reacting at 20 ℃ for 12h, and drying the solution at-20 ℃ for 48h by using a freeze dryer. And crushing the mixture into powder by using a crusher to prepare the A-DBU alginic acid proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-1, 8-diazabicycloundecan-7-ene alginic acid proton type ionic liquid precursor is put into a tube furnace to be carbonized for 1h at 500 ℃ under the Ar condition, the heating rate is 5 ℃/min, the argon flow is 200ml/min, after the temperature is reduced to the room temperature, 1.75g of a sample is weighed, 1.5g of the sample is weighed and mixed with 6g of KOH for grinding, and the proportion is that KOH/sample is 4: 1, activating the carbon material at 700 ℃ for 2 h. The temperature rise rate was 5 ℃/min and the argon flow rate was 200 ml/min. After a sample is taken out, residual KOH is washed away by using 2M HCl, the sample is washed for 3 times by using pure water, and the sample is dried for 6 hours in vacuum at 110 ℃ to obtain a target product-A-DBU-NDPs-900-4, wherein the yield is 11.96%, the nitrogen content of the obtained material is 2.88% of high nitrogen content, the graphitization degree is that ID/IG is 1.01, and the specific capacity is 76F/g under the current density of 4A/g.
Example 5 of the invention: preparation of alginic acid-tetramethylguanidine proton type ionic liquid precursor (A-TMG): 26.159g of TMG were weighed into a 250ml flask, 100ml of purified water was added, and 40g of alginic acid was added after complete mixing. Reacting at 25 ℃ for 12h, and drying the solution by a freeze dryer for 28 h. Preparing to obtain the A-TMG alginic acid proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-tetramethylguanidine proton type ionic liquid precursor is put into a tube furnace to be carbonized for 1h at 500 ℃ under the Ar condition, the heating rate is 5 ℃/min, the argon flow is 200ml/min, after the temperature is reduced to the room temperature, 1.95g of sample is weighed, 1.5g of sample is weighed, mixed and ground with 6g of KOH, and the ratio of KOH/sample is 4: 1, activating the carbon material at 900 ℃ for 2 h. The temperature rise rate was 5 ℃/min and the argon flow rate was 200 ml/min. After a sample is taken out, residual KOH is washed away by using 2M HCl, the sample is washed for 3 times by using pure water, and the sample is dried for 6 hours in vacuum at 110 ℃ to obtain a target product-A-TMG-NDPs-900-4, wherein the yield is 14.73%, the nitrogen content of the obtained material is 0.62%, the graphitization degree is that ID/IG is 1.01, and the specific capacity is 86F/g under the current density of 4A/g.
Example 6 of the invention: preparation of alginic acid-triethylamine proton type ionic liquid precursor (A-TEA): 22.982g TEA was weighed into a 250ml flask, 100ml pure water was added, and 40g alginic acid was added after complete mixing. And reacting at 25 ℃ for 48h, and drying the solution for 48h by using a freeze dryer to obtain the A-TEA proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-triethylamine proton type ionic liquid precursor is put into a tube furnace to be carbonized for 1h at 500 ℃ under the Ar condition, the heating rate is 5 ℃/min, the argon flow is 200ml/min, after the temperature is reduced to the room temperature, 1.69g of sample is weighed, 1.5g of sample is weighed, and the sample and 6g of KOH are mixed and ground, wherein the ratio of KOH/sample is 4: 1, activating the carbon material at 900 ℃ for 2 h. The temperature rise rate was 5 ℃/min and the argon flow rate was 200 ml/min. After the sample was taken out, the remaining KOH was washed away with 2M HCl, washed 3 times with pure water, and vacuum-dried at 110 ℃ for 6 hours to obtain the target product-a-TEA-NDPs-900-4 with a yield of 9.86%, a nitrogen content of the obtained material of 0.44%, a graphitization degree of ID/IG of 1.02, and a specific capacity of 91F/g at a current density of 4A/g.
Example 7 of the invention: preparing alginic acid-1-methylimidazole alginic acid proton type ionic liquid precursor (A-1-Mi): 18.646g of 1-MI were weighed into a 250ml flask, 100ml of pure water was added, and 40g of alginic acid was added after complete mixing. Reacting at 25 ℃ for 0.5h, and drying the solution by a freeze dryer for 12 h. Preparing to obtain the A-1-MI alginic acid proton type ionic liquid precursor.
Preparing a nitrogen-doped porous carbon material: 10g of alginic acid-1-methylimidazole alginic acid proton type ionic liquid precursor is put into a tube furnace and carbonized for 1h at 500 ℃ under the Ar condition, the heating rate is 5 ℃/min, the argon flow is 200ml/min, after the temperature is reduced to room temperature, 2.34g of sample is weighed, 2g of sample is weighed, mixed and ground with 8g of KOH, and the ratio of KOH/sample is 4: 1, activating the carbon material at 900 ℃ for 2 h. The temperature rise rate was 5 ℃/min and the argon flow rate was 200 ml/min. After a sample is taken out, residual KOH is washed away by using 2M HCl, the sample is washed for 3 times by using pure water, and the sample is dried for 6 hours in vacuum at 110 ℃ to obtain a target product-A-1-Mi-NDPs-900-4, wherein the yield is 17.46%, the nitrogen content of the obtained material is 1.92%, the graphitization degree is that ID/IG is 0.99, and the specific capacity is 110F/g under the current density of 4A/g.
TABLE 1 content of respective elements in Nitrogen-containing carbon Material
And (4) conclusion: alginic acid and organic bases with different structures are used for reacting to prepare proton type ionic liquids with different structures, and then the proton type ionic liquids are used as precursors to prepare carbon materials doped with different nitrogen contents. The technology provided by the patent can be used for preparing nitrogen-doped porous carbon materials with different structures.
Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.
Claims (8)
1. A method for preparing a nitrogen-doped porous carbon material by using alginic acid proton type ionic liquid as a precursor is characterized by comprising the following steps of:
1) mixing alginic acid, organic alkali and water, and reacting at 20-100 deg.C for 0.1-48 hr to synthesize alginic acid proton type ionic liquid solution;
2) drying the alginic acid proton type ionic liquid solution to obtain alginic acid proton type ionic liquid;
3) activating by using alginic acid proton type ionic liquid as a precursor through a direct carbonization method or a two-step carbonization method to obtain a nitrogen-doped carbon material product;
4) further washing the nitrogen-doped carbon material product by hydrochloric acid and pure water, and drying at 50-150 ℃ under reduced pressure to obtain a nitrogen-doped porous carbon material;
the organic base has the following structural formula:
2. the method for preparing the nitrogen-doped porous carbon material by using the alginic acid proton type ionic liquid as the precursor according to claim 1, is characterized in that: the specific chemical structure of the alginic acid is as follows:
where 50< n < 1000.
3. The method for preparing the nitrogen-doped porous carbon material by using the alginic acid proton type ionic liquid as the precursor according to claim 1 or 2, which is characterized in that: the molar ratio of the organic alkali to the alginic acid is 0.5-2: 1; the mass concentration of the formed alginic acid proton type ionic liquid in the solution is 20-80%, and the specific reaction is as follows:
4. the method for preparing the nitrogen-doped porous carbon material by using the alginic acid proton type ionic liquid as the precursor according to claim 1, is characterized in that: the drying in step 2) is at-20-Drying at 50 deg.C for 1-48 hr to obtain dried alginic acid proton type ionic liquid containing anion and cation; the anion has the structural formula:
wherein 50< n < 1000;
the cation has the structural formula:
5. the method for preparing the nitrogen-doped porous carbon material by using the alginic acid proton type ionic liquid as the precursor according to claim 1, is characterized in that: the direct carbonization method in the step 3) is specifically that the alginic acid proton type ionic liquid is transferred into a tubular furnace for heat treatment, the heating rate is 5-10 ℃/min, the inert gas is argon, the argon flow is 300mL/min, the carbonization temperature is 700-1000 ℃, and the heat preservation time is 0.5-5 h.
6. The method for preparing the nitrogen-doped porous carbon material by using the proton alginate type ionic liquid as the precursor according to claim 1, wherein the two-step carbonization method in the step 3) comprises the following steps:
a) transferring the alginic acid proton type ionic liquid powder into a tubular furnace for primary sintering, wherein the heating rate is 5-10 ℃/min, the inert gas is argon, the argon flow is 300mL/min, the carbonization temperature is 400-500 ℃, and the heat preservation time is 0.5-2 h; obtaining a preliminary sintered carbon material;
b) mixing the primary sintered carbon material obtained in the step a) with a pore-forming agent, and carrying out pore-forming while carbonizing, wherein the pore-forming agent is potassium hydroxide, and the mass ratio of the carbon material to the potassium hydroxide is 1: 1-1: 5, the heating rate is 5-10 ℃/min, the inert gas is argon, the argon flow is 300ml/min, the carbonization temperature is 700-900 ℃, and the heat preservation time is 1-5 h.
7. The method for preparing the nitrogen-doped porous carbon material by using the alginic acid proton type ionic liquid as the precursor according to claim 1, is characterized in that: in the step 4), the activated carbon material cleaning solution is 2M hydrochloric acid solution, and the amount of the hydrochloric acid solution is 5-10 times of the mass of the carbon material; the cleaning time is 1-10h, then cleaning for 2-5 times with pure water of 10-50 times of the mass, the reduced pressure drying temperature is 50-150 ℃, and the drying time is 1-5 h.
8. Use of the nitrogen-doped porous carbon material prepared according to the method of claim 1 as an electrode.
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